首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Degenerate Oligonucleotide Primed-Polymerase Chain Reaction-Based Array Comparative Genomic Hybridization for Extensive Amplicon Profiling of Breast Cancers
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Degenerate Oligonucleotide Primed-Polymerase Chain Reaction-Based Array Comparative Genomic Hybridization for Extensive Amplicon Profiling of Breast Cancers

机译:简并寡核苷酸引发的聚合酶链反应的阵列比较基因组杂交的乳腺癌的广泛扩增子分析。

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摘要

We have developed a protocol for degenerate oligonucleotide-primed-polymerase chain reaction-based array comparative genomic hybridization (array CGH) that, when combined with a laser microdissection technique, allows the analysis of cancer cell populations isolated from routine, formalin-fixed, paraffin-embedded tissue samples. Comparison of copy number changes detected by degenerate oligonucleotide-primed-polymerase chain reaction-based array CGH to those detected by conventional array CGH or fluorescence in situ hybridization, demonstrated that amplifications can be reliably detected. Using a genomic microarray containing 57 oncogenes, we screened a total of 28 breast cancer samples and obtained a detailed amplicon profile that is the most comprehensive to date in human breast cancer. The array CGH method described here will allow the genetic analysis of paraffin-embedded human cancer materials for example in the context of clinical trials.
机译:我们已经开发了用于简并寡核苷酸引发的聚合酶链反应的阵列比较基因组杂交(阵列CGH)的协议,当与激光显微切割技术结合使用时,可以分析从常规,福尔马林固定,石蜡中分离的​​癌细胞群包埋的组织样本。通过基于简并寡核苷酸引发的聚合酶链反应的阵列CGH检测到的拷贝数变化与通过常规阵列CGH或荧光原位杂交检测到的拷贝数变化的比较表明,可以可靠地检测到扩增。使用包含57个癌基因的基因组微阵列,我们筛选了28个乳腺癌样品,并获得了详细的扩增子谱,这是迄今为止人类乳腺癌中最全面的。此处描述的阵列CGH方法将允许对石蜡包埋的人类癌症材料进行遗传分析,例如在临床试验中。

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